Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.06 (G)

Chromosome 7:30969977 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB GHRHR_366+13T_G_041811

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, has 2505 sample genotypes and is associated with 1 phenotype.

Variant displays